ORPHA:217085

Mucopolysaccharidosis type 2, severe form

Also called Hunter syndrome type A, Iduronate 2-sulfatase deficiency type A, MPS2A, MPSIIA, Mucopolysaccharidosis type 2, early progressive form, Mucopolysaccharidosis type 2, neuropathic form, Mucopolysaccharidosis type 2A, Mucopolysaccharidosis type II, severe form, Mucopolysaccharidosis type IIA

Body system

Bone diseases

Inheritance pattern

X-linked recessive

Typical age of onset

Childhood

Estimated prevalence

1-9 / 1 000 000 (Europe)

Rarity class

1-9 / 1 000 000

ORPHA:217085 is classified under "Bone diseases" in the Orphanet nomenclature.